Canonical Allele Identifier: CA970008129

Gene: UNC13C

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.54615050G>C , CM000677.2:g.54615050G>C	GRCh38
NC_000015.9:g.54907248G>C , CM000677.1:g.54907248G>C	GRCh37
NC_000015.8:g.52694540G>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000260323.16:c.6107-7277G>C MANE Select	ENSP00000260323.11:n.6107-7277G>C
ENST00000647821.1:c.6101-7277G>C	ENSP00000497525.1:n.6101-7277G>C
ENST00000260323.15:c.6107-7277G>C	ENSP00000260323.11:n.6107-7277G>C
ENST00000539562.6:c.-132+5606G>C	ENSP00000443886.2:n.-132+5606G>C
ENST00000560537.1:c.-132+3406G>C	ENSP00000456350.1:n.-132+3406G>C
NM_001080534.1:c.6107-7277G>C	NP_001074003.1:n.6107-7277G>C
XM_005254394.3:c.6107-7277G>C	XP_005254451.1:n.6107-7277G>C
XM_005254395.3:c.6029-7277G>C	XP_005254452.1:n.6029-7277G>C
NM_001080534.2:c.6107-7277G>C	NP_001074003.1:n.6107-7277G>C
NM_001329919.1:c.6101-7277G>C	NP_001316848.1:n.6101-7277G>C
XM_005254394.5:c.6107-7277G>C	XP_005254451.1:n.6107-7277G>C
XM_017022220.1:c.6107-7277G>C	XP_016877709.1:n.6107-7277G>C
XM_017022221.1:c.6107-7277G>C	XP_016877710.1:n.6107-7277G>C
XM_017022222.1:c.6107-7277G>C	XP_016877711.1:n.6107-7277G>C
XM_017022223.1:c.6101-7277G>C	XP_016877712.1:n.6101-7277G>C
XM_017022225.1:c.3005-7277G>C	XP_016877714.1:n.3005-7277G>C
XR_001751291.1:n.12286-7277G>C
NM_001329919.2:c.6101-7277G>C	NP_001316848.1:n.6101-7277G>C
NM_001080534.3:c.6107-7277G>C MANE Select	NP_001074003.1:n.6107-7277G>C